Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Denis Pierron
Whole Mitochondrial Genome Screening in Maternally Inherited Non-Syndromic Hearing Impairment Using a Microarray Resequencing Mitochondrial DNA Chip
European Journal of Human Genetics
Genetics
Related publications
Frequency of Mitochondrial Mutations in Non-Syndromic Hearing Loss as Well as Possibly Responsible Variants Found by Whole Mitochondrial Genome Screening
Journal of Human Genetics
Genetics
Nuclear-Mitochondrial DNA Segments Resemble Paternally Inherited Mitochondrial DNA in Humans
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Maternally Transmitted Mitochondrial DNA Mutations Can Reduce Lifespan
Scientific Reports
Multidisciplinary
Modifier Locus for Mitochondrial DNA Disease: Linkage and Linkage Disequilibrium Mapping of a Nuclear Modifier Gene for Maternally Inherited Deafness
Genetics in Medicine
Medicine
Genetics
Y-Linked Inheritance of Non-Syndromic Hearing Impairment in a Large Chinese Family
Journal of Medical Genetics
Genetics
DFNB1 Non-Syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
Frontiers in Molecular Neuroscience
Molecular Neuroscience
Molecular Biology
Cellular
Figure 2: Whole Genome Resequencing Analysis.
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
